These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
114 related articles for article (PubMed ID: 11697955)
1. Thermodynamic versus kinetic products of DNA alkylation as modeled by reaction of deoxyadenosine. Veldhuyzen WF; Shallop AJ; Jones RA; Rokita SE J Am Chem Soc; 2001 Nov; 123(45):11126-32. PubMed ID: 11697955 [TBL] [Abstract][Full Text] [Related]
2. Alkylation of 2'-deoxynucleosides and DNA by quinone methides derived from 2,6-di-tert-butyl-4-methylphenol. Lewis MA; Yoerg DG; Bolton JL; Thompson JA Chem Res Toxicol; 1996 Dec; 9(8):1368-74. PubMed ID: 8951242 [TBL] [Abstract][Full Text] [Related]
3. Time-dependent evolution of adducts formed between deoxynucleosides and a model quinone methide. Weinert EE; Frankenfield KN; Rokita SE Chem Res Toxicol; 2005 Sep; 18(9):1364-70. PubMed ID: 16167827 [TBL] [Abstract][Full Text] [Related]
4. 2'-Deoxyguanosine reacts with a model quinone methide at multiple sites. Veldhuyzen WF; Lam YF; Rokita SE Chem Res Toxicol; 2001 Sep; 14(9):1345-51. PubMed ID: 11559052 [TBL] [Abstract][Full Text] [Related]
5. Oxidative quenching of quinone methide adducts reveals transient products of reversible alkylation in duplex DNA. McCrane MP; Hutchinson MA; Ad O; Rokita SE Chem Res Toxicol; 2014 Jul; 27(7):1282-93. PubMed ID: 24896651 [TBL] [Abstract][Full Text] [Related]
6. Selective N1-alkylation of 2'-deoxyguanosine with a quinolinyl quinone methide. Zhou Q; Xu T; Mangrum JB Chem Res Toxicol; 2007 Aug; 20(8):1069-74. PubMed ID: 17630703 [TBL] [Abstract][Full Text] [Related]
7. Oxidation of eugenol to form DNA adducts and 8-hydroxy-2'-deoxyguanosine: role of quinone methide derivative in DNA adduct formation. Bodell WJ; Ye Q; Pathak DN; Pongracz K Carcinogenesis; 1998 Mar; 19(3):437-43. PubMed ID: 9525278 [TBL] [Abstract][Full Text] [Related]
9. Selective Alkylation of C-Rich Bulge Motifs in Nucleic Acids by Quinone Methide Derivatives. Lönnberg T; Hutchinson M; Rokita S Chemistry; 2015 Sep; 21(37):13127-36. PubMed ID: 26220692 [TBL] [Abstract][Full Text] [Related]
10. Isolation and Rationale for the Formation of Isomeric Decarbamoylmitomycin C- N Zacarias O; Aguilar W; Paz MM; Tsukanov S; Zheng M; Cheng SY; Pradhan P; Champeil E Chem Res Toxicol; 2018 Aug; 31(8):762-771. PubMed ID: 30035537 [TBL] [Abstract][Full Text] [Related]
11. Modeling H-bonding and solvent effects in the alkylation of pyrimidine bases by a prototype quinone methide: a DFT study. Freccero M; Di Valentin C; Sarzi-Amadè M; J Am Chem Soc; 2003 Mar; 125(12):3544-53. PubMed ID: 12643716 [TBL] [Abstract][Full Text] [Related]
12. Sequence-specific delivery of a quinone methide intermediate to the major groove of DNA. Zhou Q; Pande P; Johnson AE; Rokita SE Bioorg Med Chem; 2001 Sep; 9(9):2347-54. PubMed ID: 11553475 [TBL] [Abstract][Full Text] [Related]
13. Selectivity of purine alkylation by a quinone methide. Kinetic or thermodynamic control? Freccero M; Gandolfi R; Sarzi-Amadè M J Org Chem; 2003 Aug; 68(16):6411-23. PubMed ID: 12895079 [TBL] [Abstract][Full Text] [Related]
14. Identification and characterization of novel stable deoxyguanosine and deoxyadenosine adducts of benzo[a]pyrene-7,8-quinone from reactions at physiological pH. Balu N; Padgett WT; Lambert GR; Swank AE; Richard AM; Nesnow S Chem Res Toxicol; 2004 Jun; 17(6):827-38. PubMed ID: 15206904 [TBL] [Abstract][Full Text] [Related]
18. Predicted exocyclic amino group alkylation of 2'-deoxyadenosine and 2'-deoxyguanosine by the isopropyl cation. Blans P; Fishbein JC Chem Res Toxicol; 2000 Jun; 13(6):431-5. PubMed ID: 10858315 [TBL] [Abstract][Full Text] [Related]
19. Solution structure of a trans-opened (10S)-dA adduct of (+)-(7S,8R,9S,10R)-7,8-dihydroxy-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene in a fully complementary DNA duplex: evidence for a major syn conformation. Pradhan P; Tirumala S; Liu X; Sayer JM; Jerina DM; Yeh HJ Biochemistry; 2001 May; 40(20):5870-81. PubMed ID: 11352722 [TBL] [Abstract][Full Text] [Related]
20. Structure-activity study on the quinone/quinone methide chemistry of flavonoids. Awad HM; Boersma MG; Boeren S; van Bladeren PJ; Vervoort J; Rietjens IM Chem Res Toxicol; 2001 Apr; 14(4):398-408. PubMed ID: 11304128 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]